Abstract
A new synthetic protocol that combines the advantages
offered by eco-friendly solvent-free reactions
and sequential transformations is reported. This strategy
offers straightforward access to benzo[c]chromenes and
benzo[b]furans from commercially available starting materials.
This two-step, one-pot strategy consists of an Au-catalyzed
hydrophenoxylation process followed by Pd-catalyzed
CH activation or Mizoroki–Heck reactions. The selectivity
of the process towards CH activation or Mizoroki–
Heck reaction can be easily tuned.
offered by eco-friendly solvent-free reactions
and sequential transformations is reported. This strategy
offers straightforward access to benzo[c]chromenes and
benzo[b]furans from commercially available starting materials.
This two-step, one-pot strategy consists of an Au-catalyzed
hydrophenoxylation process followed by Pd-catalyzed
CH activation or Mizoroki–Heck reactions. The selectivity
of the process towards CH activation or Mizoroki–
Heck reaction can be easily tuned.
Original language | English |
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Pages (from-to) | 13507 – 13510 |
Number of pages | 4 |
Journal | Chemistry - A European Journal |
Volume | 20 |
Early online date | 28 Aug 2014 |
DOIs | |
Publication status | Published - 2014 |